Job Description
About Our Client
Our client is a global biopharmaceutical company focused on discovering and delivering innovative medicines that solve serious health issues. With a strong commitment to research, development, and regulatory excellence, the company prioritizes patient outcomes and scientific advancement.
Job Description
- Manage submissions for new product registrations and post-approval variations in line with local regulatory requirements and company timelines
- Collaborate closely with internal stakeholders to prepare and maintain regulatory documentation
- Respond to health authority queries and deficiency letters within required timelines
- Monitor and interpret updates from global headquarters to ensure loc...
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